Indoco Remedies Ltd – Walk-In Interview for Multiple Positions in Production / Packing / QC / QA / Liquid Manufacturing & Packing on 20th Aug’ 2023

Indoco Remedies Ltd – Walk-In Interview for Multiple Positions in Production / Packing / QC / QA / Liquid Manufacturing & Packing on 20th Aug’ 2023

 

Indoco Remedies Ltd., is a leading pharma Company with global presence in 55 countries and international regulatory approvals including USFDA and UKMHRA. WALK-IN-INTERVIEWS For our tablet manufacturing facility in Goa.

  • OFFICER / SR. OFFICER / EXECUTIVE – PRODUCTION
  • SR OFFICER / JR EXECUTIVE – (LIQUID MFG/PKG)
  • OFFICER PACKING
  • QC-ANALYST,
  • QA – QMS,
  • QA – INVESTIGATOR,
  • QA – IPQA
  • VENUE: Goa Woodlands Hotel Rua Miguel de Loyola Furtado, Opp. City Bus Stand, Margao, Goa 403601
  • DATE: Sunday, 20/08/2023
  • TIME: 10:30 am to 4:30 pm

CONTACT DETAILS:

Ms. Deepika Gayak – HR Tel: 0832-6624109  / hrd1@indoco.com
Mr. Manjesh Nayak – HR Mob.: Tel: 0832-6721628  / hrd3@indoco.com

Job Description:

OFFICER / SR. OFFICER/EXECUTIVE – PRODUCTION:

  • Qualification : B. Pharm / M. Pharm
  • Job Profile : 1 to 9 years’ experience in granulation, compression & coating areas for regulated market. FDA approval in tablet manufacturing would be preferred. Having machine exposure of FETTE, Sejong for compression and FBD, FBE, RMG for Granulation.

 

SR. OFFICER / Jr. EXECUTIVE – (Liquid MFG/PKG):

  • Qualification : B. Pharm / M. Pharm
  • Job Profile : 2 to 5 years’ experience in Liquid Manufacturing and Liquid Packing departments to manage routine manufacturing and packing activities. Experience in handling of Track and Trace system, coordination of shifts and batch reconciliation.

 

OFFICER – PACKING :

  • Qualification : B. Pharm / M. Pharm
  • Job Profile : 2 to 4 years’ of experience in tablet packing department to manage routine packing activities on high speed blister packaging lines equipped with cartonators and bottle packing line. Experience in handling Track and Trace system, coordination of shifts and batch reconciliation.

 

QC – ANALYST :

  • Qualification : BSC / MSC in (Chemistry/ Analytical)
  • Job Profile : 3 to 7 years’ experience in stability, validation, finished product, in process, raw material and GLP. Software knowledge of Empower, Lab Solution & Tiamo Caliber LIMS. Experience in handling instruments like HPLC, UV, IR, KF GC, Malvern. Exposure of regulatory audits like USFDA, MHRA, EU, WHO.

 

QA-QMS :

  • Qualification : B. Pharm / M. Pharm
  • Job Profile : 4 to 5 years’ experience in handling change controls, deviations, market complaints, CAPA. Review of quality risk management. Preparation/review of SOPs. To carry out activities related to training. Candidate must have experience in regulatory plants.

 

QA-INVESTIGATOR:

  • Qualification : B. Pharm / M. Pharm
  • Job Profile : 7 to 8 years’ experience in handling market complaints, investigation related to deviations and CAPA. Preparation/Review of APQR. Quality alert notification, field alert and handling product recall related activities. To carry out activities related to training. Candidate must have experience in regulatory plants.

 

QA-IPQA:

  • Qualification : B. Pharm / M. Pharm
  • Job Profile : 2 to 3 years’ experience in handling of IPQA related activities like Line clearance, sampling, in process checks, batch record review, QA rounds, batch release (Semi Finished), material verification, swab sampling, IPQC instrument handling, etc. Candidate must have experience in regulatory plants..

Above positions are for candidates to work in all shifts

For job description please click on the below linkhttps://www.indoco.com/job-description/Goa-Walk-in-drive-Aug2023.pdf

Job Category: pharma
Job Type: Full Time
Job Location: Goa

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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